Electrochemical synthesis methods were developed to produce CuBi2O4, a promising p-type oxide for use in solar water splitting, as high surface area electrodes with uniform coverage. These methods involved electrodepositing nanoporous Cu/Bi films with a Cu:Bi ratio of 1:2 from dimethyl sulfoxide or ethylene glycol solutions, and thermally oxidizing them to CuBi2O4 at 450 °C in air. Ag-doped CuBi2O4 electrodes were also prepared by adding a trace amount of Ag+ in the plating medium and codepositing Ag with the Cu/Bi films. In the Ag-doped CuBi2O4, Ag+ ions substitutionally replaced Bi3+ ions and increased the hole concentration in CuBi2O4. As a result, photocurrent enhancements for both O2 reduction and water reduction were achieved. Furthermore, while undoped CuBi2O4 electrodes suffered from anodic photocorrosion during O2 reduction due to poor hole transport, Ag-doped CuBiO4 effectively suppressed anodic photocorrosion. The flat-band potentials of CuBi2O4 and Ag-doped CuBi2O4 electrodes prepared in this study were found to be more positive than 1.3 V vs RHE in a 0.1 M NaOH solution (pH 12.8), which make these photocathodes highly attractive for use in solar hydrogen production. The optimized CuBi2O4/Ag-doped CuBi2O4 photocathode showed a photocurrent onset for water reduction at 1.1 V vs RHE, achieving a photovoltage higher than 1 V for water reduction. The thermodynamic feasibility of photoexcited electrons in the conduction band of CuBi2O4 to reduce water was also confirmed by detection of H2 during photocurrent generation. This study provides new understanding for constructing improved CuBi2O4 photocathodes by systematically investigating photocorrosion as well as photoelectrochemical properties of high-quality CuBi2O4 and Ag-doped CuBi2O4 photoelectrodes for photoreduction of both O2 and water.